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Experience of working in medical affairs in the pharmaceutical industry * Therapeutic area experience of neurological disorders would be a plus * Possible experienced in vendor medical communication ...
Hold a Scientific Degree. * 1 years' experience within Pharmaceutical or Medical Device Regulatory Affairs. * Expert organisation skills * Strong written and verbal communication skills. Benefits for ...
Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...
... Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an ... trials and medical products. * Contributing regulatory guidance in order to enhance product ...
Serve as a local Medical Affairs representative in standing and project-based cross-functional teams * Provide medical and scientific expertise supporting cross-functional projects (e.g., materials ...
... trials and medical products. * Contributing regulatory guidance in order to enhance product ... Centralised Regulatory Affairs experience * Strong strategic experience within Regulatory Affairs
As Associate Director, Global Regulatory Affairs Strategy, you will be responsible for: * Lead the ... Minimum 7 years Regulatory experience, with 4+ years in industry / US Medical Device * Experience ...
... Medical Device Regulations, International Standards, and Customer Requirements and that this is ... Responsibilities · Responsible for maintaining and supporting the promotion of regulatory affairs ...
The Natural Doctor clinic on Harley Street is offering an exciting sessional Medical Practitioner vacancy for a professional with an interest in BHRT menopause management, Functional Medicine, and ...
Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading global drug development organization. We are seeking a motivated individual with substantial experience in Medical Device Regulation, particularly in the areas of combination pr...
Associate Director, Medical Affairs. If you're a strategic innovator within Medical Affairs, this is an opportunity for you. ...
Great mix of global and EU med affairs and commercial work, across an established and growing osteoporosis account. ...
Extensive experience in Regulatory Affairs with experience acting as therapeutic area European Regulatory Affairs lead, defining and implement regulatory strategies and executional plans. Define and advise the GRT on regional considerations in developing creative regulatory strategy, lead develop...
CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Regulatory Affairs Associate Role:. Experience in a Regulatory Affairs role in CMC, including preparation of submissions to Agencies and fami...
Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...
If you would like an exploratory chat about this role or the other opportunities available, please get in touch via elaine@medicaltalent. ...
Remote Senior Regulatory Medical Writer working through an FSP model for a Global Oncology focused Pharmaceutical Company. The Principal Medical Writer I is responsible for developing clinical documents for submissions to regulatory authorities globally. Oversees the medical writing activities of...
VP, Medical Director, CMC Affinity - UK. We are CMC Affinity, and we are hiring for an VP, Medical Director to join our global team, based in the UK. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, united by a healthy obsession with creatin...
Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...
Principal Medical Writer Opportunity. Join a dynamic and ambitious truly independent agency as a Principal Medical Writer and immerse yourself in diverse, exciting med affairs, meded and omnichannel projects. ...
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to operate as a Regulatory Lead, providing centralised regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved. A global pharmaceutical c...
The role will encompass a large percentage of medical affairs work, as well as some promotional (and no publications!) The ideal candidate will have a blend of creative, visual experience, as well as the knowledge and confidence to work across high science accounts/projects. ...
Senior Regulatory Affairs Specialist who will be responsible for planning, creating, and implementing solutions for regulatory registration and release of products for distribution into specific geographies. Senior Regulatory Affairs Specialist – Medical Devices & IVD’s. Minimum of 4 to 5 years p...
An opportunity for a Chemical Regulatory Affairs Specialist to join a global chemical trade association as manager of global regulatory intelligence. This is a key new hire within the Scientific and Regulatory Affairs team – you will provide regulatory support to the chemicals management and Gove...
